Tru-Vu Wrist Positioning Aid Multi-Center Implementation Within NLHS
2026年5月13日 更新者：Emily Lalone、Western University
This study has two primary aims: 1) to determine whether a novel wrist x-ray positioning aid can be implemented within 3 different healthcare centers in Newfoundland and Labrador, and 2) to determine the ability of the tool to improve patient positioning in wrist x-rays. It will also learn about the number of repeat x-rays required with or without the use of the tool and radiographer confidence. The main questions it aims to answer are:
- Will the implementation of the Tru-Vu differ between an urban health center, rural clinic, and remote regional hospital?
- Can the Tru-Vu improve the positioning procedure for radiographers performing wrist x-rays, resulting with more useful x-rays.
Researchers will compare x-rays before and after the implementation of the tool as well as between centers.
Technologist participants will:
- Use the tool during the positioning procedure for wrist x-rays.
- Provide feedback regarding tool use and perceived implementation barriers and facilitators.
研究概览
研究类型
介入性
注册 (估计的)
1800
阶段
- 第三阶段
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习联系方式
- 姓名：Emily Lalone, PhD
- 电话号码：88243 519-661-2111
- 邮箱：emily.lalone@uwo.ca
学习地点
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Labrador
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Happy Valley-Goose Bay、Labrador、加拿大、A0P1C0
- Labrador Health Centre
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接触：
- Emily Lalone, PhD
- 电话号码：88243 519-661-2111
- 邮箱：emily.lalone@uwo.ca
-
-
Newfoundland and Labrador
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Norris Point、Newfoundland and Labrador、加拿大、A8A3L1
- Bonne Bay Health Centre
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接触：
- Emily Lalone, PhD
- 电话号码：88243 519-661-2111
- 邮箱：emily.lalone@uwo.ca
-
St. John's、Newfoundland and Labrador、加拿大、A1B3V6
- Health Sciences Centre
-
接触：
- Emily Lalone, PhD
- 电话号码：88243 519-661-2111
- 邮箱：emily.lalone@uwo.ca
-
-
参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Must be 18 years of age or older
- Must be proficient in English (reading/writing)
- Must have been referred for wrist imaging at one of the following healthcare centers: Health Sciences Center (St. John's, NL), Bonne Bay Health Center (Norris Point, NL), or Labrador Health Center (Happy Valley-Goose Bay, NL).
Exclusion Criteria:
- Incapable of providing informed consent
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：其他
- 分配：非随机化
- 介入模型：并行分配
- 屏蔽：单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的：Urban hospital
Radiographs will be retrospectively collected and compared to radiographs captured after the implementation of the tool.
Additional radiographs will be collected over a 6-month follow-up period.
|
A positioning aid and training videos for wrist x-rays
|
|
实验性的：Rural health center
Radiographs will be retrospectively collected and compared to radiographs captured after the implementation of the tool.
Additional radiographs will be collected over a 6-month follow-up period.
|
A positioning aid and training videos for wrist x-rays
|
|
实验性的：Regional remote hospital
Radiographs will be retrospectively collected and compared to radiographs captured after the implementation of the tool.
Additional radiographs will be collected over a 6-month follow-up period.
|
A positioning aid and training videos for wrist x-rays
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Radiograph grading score
大体时间：Radiographs will be collected retrospectively 4 months prior to implementation and 6 months prospectively after the implementation of the tool.
|
Radiographs collected retrospectively and prospectively will be graded by a radiologist and radiographer
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Radiographs will be collected retrospectively 4 months prior to implementation and 6 months prospectively after the implementation of the tool.
|
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Tool adoption (and associated implementation outcomes)
大体时间：The survey will be administered 6 months after the implementation of the tool and training.
|
A survey will collect perceived tool use and other perceived implementation outcomes (including fidelity, appropriateness, acceptability, and adoption).
|
The survey will be administered 6 months after the implementation of the tool and training.
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Sustainability
大体时间：6 months after the conclusion of the implementation period
|
Post-follow up survey will be conducted 6 months after the end of the implementation period and will collect perceived tool use.
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6 months after the conclusion of the implementation period
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Repeated radiographs
大体时间：Repeat radiographs will be collected and compared 4 months retrospectively prior to implementation and 6 months after the start of implementation.
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Document the number of repeat radiographs captured.
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Repeat radiographs will be collected and compared 4 months retrospectively prior to implementation and 6 months after the start of implementation.
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年6月14日
初级完成 (估计的)
2027年2月1日
研究完成 (估计的)
2027年9月1日
研究注册日期
首次提交
2026年5月5日
首先提交符合 QC 标准的
2026年5月5日
首次发布 (实际的)
2026年5月12日
研究记录更新
最后更新发布 (实际的)
2026年5月18日
上次提交的符合 QC 标准的更新
2026年5月13日
最后验证
2026年5月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.